Multi-unit Abutment Plus
K-Number: K161416 · 2017-03-16
ApplicantNobel Biocare AB
Decision Date2017-03-16
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Multi-unit Abutment Plus is a medical device manufactured by Nobel Biocare AB. It received FDA 510(k) clearance on 2017-03-16 under approval number K161416. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Multi-unit Abutment Plus?
Multi-unit Abutment Plus is a medical device that received FDA 510(k) clearance on 2017-03-16. It is manufactured by Nobel Biocare AB. The 510(k) number is K161416.
When was Multi-unit Abutment Plus approved by the FDA?
Multi-unit Abutment Plus received FDA 510(k) clearance on 2017-03-16, under approval number K161416.
What company makes Multi-unit Abutment Plus?
Multi-unit Abutment Plus is manufactured by Nobel Biocare AB.
What is the FDA product code for Multi-unit Abutment Plus?
The FDA product code for Multi-unit Abutment Plus is NHA.
Related Clinical Trials
Other Devices by Nobel Biocare AB
Related Devices (Code: NHA)
K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd.
K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG
K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A.
K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd.
K161435Temporary Snap AbutmentNobel Biocare AB
K160786RODO Abutment SystemRodo Medical, Inc.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.